Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06869512

Cooperative Extension and Cancer Survivorship: Supportive Care Via Cooperative Extension Services (SUCCESS)

Led by University of Oklahoma · Updated on 2025-06-26

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Oklahoma

Lead Sponsor

O

Oklahoma State University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the SUCCESS program, a cancer survivorship initiative delivered through Cooperative Extension services, to see if it is practical and can improve health outcomes for adults who have completed active cancer treatment. The study aims to assess the program's feasibility, participant acceptance, and its preliminary effects on health-related quality of life and other psychosocial factors. Additionally, the trial examines changes in gene expression related to stress response in a subset of participants. The SUCCESS program consists of six weekly group education sessions. Each session includes 25 minutes of teaching and discussion, 25 minutes of facilitated support group time, and 10 minutes of group exercise. This is a single-arm trial without a comparison group, focusing on delivering the program and collecting data over a six-week period. Participants will complete surveys and join Zoom sessions before starting and after finishing the program to provide data on various health outcomes such as diet quality, physical function, mental health symptoms, social factors, financial toxicity, and gene expression changes. Researchers will monitor session delivery, participant attendance, adherence to the program, and acceptability ratings. The total participation duration is approximately seven to eight weeks, including follow-up assessments.

CONDITIONS

Brief Title

Cooperative Extension and Cancer Survivorship

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Previous adult-diagnosed cancer
  • Completed active cancer treatment
  • Not currently receiving active cancer treatment, but hormonal therapy is allowed
  • Ability to attend group sessions
  • Residency in Oklahoma
Not Eligible

You will not qualify if you...

  • Receiving palliative or hospice care
  • Medical or surgical history preventing participation
  • Positive Physical Activity Readiness Questionnaire+ (PAR-Q+) without doctor's approval to participate

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - 6 weeks

Participants attend the SUCCESS program which includes 6 weekly group education sessions. Each session consists of 25 minutes of didactic and discussion-based lecture, 25 minutes of facilitated support group, and 10 minutes of brief group-based exercise.

Weekly visits for 6 weeks

Trial Site Locations

Total: 1 location

1

University of Oklahoma

Tulsa, Oklahoma, United States, 74135

Actively Recruiting

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Research Team

A

Ashlea C Braun, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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Published Research Related To This Trial

Hiding in plain sight: Cooperative Extension as an underutilized approach to improving cancer survivorship outcomes in underserved populations.

Olivia Pitasi, Deana Hildebrand, Rachel Liebe...

https://pubmed.ncbi.nlm.nih.gov/39388009